Other mutations in this stock |
Total: 111 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310034C09Rik |
G |
C |
16: 88,556,053 (GRCm39) |
S89T |
probably benign |
Het |
4930522L14Rik |
C |
G |
5: 109,884,616 (GRCm39) |
C414S |
probably damaging |
Het |
4930553M12Rik |
G |
A |
4: 88,786,411 (GRCm39) |
T69I |
unknown |
Het |
4930553M12Rik |
T |
A |
4: 88,786,412 (GRCm39) |
T69S |
unknown |
Het |
Apobr |
G |
A |
7: 126,186,288 (GRCm39) |
E600K |
probably benign |
Het |
Armc8 |
C |
A |
9: 99,387,361 (GRCm39) |
R419L |
probably damaging |
Het |
Ash1l |
T |
A |
3: 88,892,726 (GRCm39) |
M1535K |
probably benign |
Het |
Atf7ip2 |
A |
G |
16: 10,058,509 (GRCm39) |
E316G |
probably null |
Het |
Atp2a1 |
G |
A |
7: 126,047,897 (GRCm39) |
R638* |
probably null |
Het |
Atp8b4 |
A |
T |
2: 126,216,430 (GRCm39) |
I672N |
probably damaging |
Het |
Atrn |
T |
C |
2: 130,799,916 (GRCm39) |
V431A |
probably benign |
Het |
Babam1 |
T |
C |
8: 71,851,084 (GRCm39) |
S116P |
probably damaging |
Het |
Ccdc142 |
T |
C |
6: 83,079,203 (GRCm39) |
L180P |
probably damaging |
Het |
Cd52 |
T |
C |
4: 133,821,048 (GRCm39) |
|
probably benign |
Het |
Cdk17 |
T |
C |
10: 93,053,881 (GRCm39) |
L125P |
probably damaging |
Het |
Ckap5 |
A |
G |
2: 91,396,090 (GRCm39) |
D531G |
probably benign |
Het |
Cntn5 |
G |
T |
9: 9,748,420 (GRCm39) |
P487Q |
probably damaging |
Het |
Crispld1 |
C |
T |
1: 17,819,860 (GRCm39) |
T286I |
probably benign |
Het |
Crtap |
T |
C |
9: 114,209,036 (GRCm39) |
Y336C |
probably damaging |
Het |
Ctu2 |
T |
A |
8: 123,205,891 (GRCm39) |
I213K |
probably benign |
Het |
Dmac2l |
A |
G |
12: 69,787,828 (GRCm39) |
Q88R |
probably damaging |
Het |
Dsc3 |
A |
G |
18: 20,113,743 (GRCm39) |
F393S |
possibly damaging |
Het |
Dsg2 |
T |
A |
18: 20,712,218 (GRCm39) |
I118N |
probably damaging |
Het |
Dstyk |
T |
A |
1: 132,391,113 (GRCm39) |
M838K |
probably damaging |
Het |
Elmo3 |
T |
C |
8: 106,035,305 (GRCm39) |
V450A |
probably damaging |
Het |
Eml5 |
A |
C |
12: 98,776,864 (GRCm39) |
F1417C |
probably damaging |
Het |
Enam |
T |
A |
5: 88,640,779 (GRCm39) |
M147K |
probably benign |
Het |
Entpd1 |
T |
C |
19: 40,725,227 (GRCm39) |
Y409H |
probably damaging |
Het |
Extl1 |
C |
A |
4: 134,098,355 (GRCm39) |
E225D |
probably benign |
Het |
Fbn2 |
A |
G |
18: 58,186,065 (GRCm39) |
V1761A |
possibly damaging |
Het |
Fsip2 |
A |
T |
2: 82,820,615 (GRCm39) |
L5449F |
possibly damaging |
Het |
Gabra5 |
G |
A |
7: 57,138,763 (GRCm39) |
T95I |
probably damaging |
Het |
Gal3st2c |
C |
T |
1: 93,937,173 (GRCm39) |
Q373* |
probably null |
Het |
Gbp5 |
A |
C |
3: 142,209,593 (GRCm39) |
T180P |
probably damaging |
Het |
Glb1 |
T |
C |
9: 114,266,892 (GRCm39) |
L212P |
probably damaging |
Het |
Gm11596 |
A |
T |
11: 99,683,789 (GRCm39) |
C110* |
probably null |
Het |
Gpat2 |
T |
C |
2: 127,275,682 (GRCm39) |
F487L |
probably damaging |
Het |
Hsph1 |
A |
T |
5: 149,554,951 (GRCm39) |
H110Q |
probably damaging |
Het |
Ikbke |
C |
A |
1: 131,201,211 (GRCm39) |
V176L |
probably damaging |
Het |
Ildr2 |
T |
C |
1: 166,096,895 (GRCm39) |
V38A |
probably damaging |
Het |
Inpp4a |
G |
T |
1: 37,426,827 (GRCm39) |
C326F |
probably damaging |
Het |
Irak2 |
T |
A |
6: 113,649,788 (GRCm39) |
V141D |
probably benign |
Het |
Jade1 |
G |
A |
3: 41,559,143 (GRCm39) |
R408Q |
probably benign |
Het |
Jmjd7 |
C |
A |
2: 119,860,601 (GRCm39) |
|
probably null |
Het |
Kdm7a |
C |
T |
6: 39,145,884 (GRCm39) |
V348I |
possibly damaging |
Het |
Kif20a |
A |
G |
18: 34,758,657 (GRCm39) |
D42G |
possibly damaging |
Het |
Klhl7 |
A |
T |
5: 24,305,861 (GRCm39) |
M37L |
probably benign |
Het |
Krt5 |
A |
G |
15: 101,620,794 (GRCm39) |
I151T |
probably damaging |
Het |
Krtap1-5 |
T |
C |
11: 99,471,644 (GRCm39) |
I50V |
probably benign |
Het |
Letm1 |
A |
AG |
5: 33,926,859 (GRCm39) |
|
probably null |
Het |
Lrrc71 |
C |
T |
3: 87,652,828 (GRCm39) |
W148* |
probably null |
Het |
Lsmem1 |
GTACATACATACATACATACATACATACA |
GTACATACATACATACATACATACATACATACA |
12: 40,235,260 (GRCm39) |
|
probably null |
Het |
Map1a |
T |
A |
2: 121,132,426 (GRCm39) |
S843T |
probably damaging |
Het |
Map1s |
T |
A |
8: 71,363,608 (GRCm39) |
D48E |
probably damaging |
Het |
Mast4 |
A |
G |
13: 102,871,983 (GRCm39) |
F2462L |
possibly damaging |
Het |
Mettl21e |
T |
A |
1: 44,249,398 (GRCm39) |
Y86F |
probably benign |
Het |
Myh6 |
A |
T |
14: 55,190,411 (GRCm39) |
D1035E |
probably damaging |
Het |
Naip6 |
C |
T |
13: 100,436,367 (GRCm39) |
D719N |
probably damaging |
Het |
Nat8f2 |
T |
G |
6: 85,845,239 (GRCm39) |
H41P |
probably benign |
Het |
Ncam1 |
T |
A |
9: 49,454,319 (GRCm39) |
Q597L |
possibly damaging |
Het |
Nek1 |
T |
A |
8: 61,481,730 (GRCm39) |
I215K |
probably damaging |
Het |
Nol11 |
A |
T |
11: 107,071,881 (GRCm39) |
S237R |
probably benign |
Het |
Npr2 |
T |
C |
4: 43,648,166 (GRCm39) |
F870S |
probably damaging |
Het |
Nsd1 |
T |
C |
13: 55,408,210 (GRCm39) |
Y1285H |
probably damaging |
Het |
Nup93 |
C |
T |
8: 95,023,108 (GRCm39) |
Q229* |
probably null |
Het |
Or4a15 |
C |
T |
2: 89,193,447 (GRCm39) |
E109K |
probably damaging |
Het |
Or7g12 |
G |
A |
9: 18,900,099 (GRCm39) |
A272T |
probably benign |
Het |
Pappa |
T |
A |
4: 65,099,186 (GRCm39) |
Y568* |
probably null |
Het |
Parva |
A |
G |
7: 112,159,274 (GRCm39) |
D180G |
possibly damaging |
Het |
Pask |
C |
T |
1: 93,249,019 (GRCm39) |
A794T |
probably benign |
Het |
Pax1 |
T |
A |
2: 147,207,802 (GRCm39) |
C225S |
probably damaging |
Het |
Pde4dip |
T |
A |
3: 97,795,835 (GRCm39) |
E51V |
possibly damaging |
Het |
Pde6c |
A |
T |
19: 38,150,777 (GRCm39) |
H562L |
probably damaging |
Het |
Pet100 |
T |
G |
8: 3,672,355 (GRCm39) |
L14R |
probably damaging |
Het |
Pfkfb2 |
T |
C |
1: 130,626,460 (GRCm39) |
T438A |
probably benign |
Het |
Pira2 |
A |
T |
7: 3,847,344 (GRCm39) |
L115Q |
probably damaging |
Het |
Polr2d |
T |
A |
18: 31,929,132 (GRCm39) |
L127Q |
probably damaging |
Het |
Prkd1 |
A |
G |
12: 50,536,694 (GRCm39) |
V130A |
possibly damaging |
Het |
Psd3 |
T |
C |
8: 68,417,003 (GRCm39) |
D45G |
probably damaging |
Het |
Ptpn13 |
A |
G |
5: 103,703,999 (GRCm39) |
T1344A |
probably benign |
Het |
Ptpn6 |
T |
A |
6: 124,701,947 (GRCm39) |
H406L |
probably benign |
Het |
Ric1 |
A |
T |
19: 29,510,652 (GRCm39) |
S78C |
probably damaging |
Het |
Ric1 |
G |
A |
19: 29,510,653 (GRCm39) |
S78N |
probably damaging |
Het |
Scgb1b2 |
G |
T |
7: 30,991,188 (GRCm39) |
|
probably benign |
Het |
Senp7 |
A |
G |
16: 55,990,169 (GRCm39) |
H639R |
probably benign |
Het |
Sgtb |
A |
T |
13: 104,260,767 (GRCm39) |
D72V |
probably damaging |
Het |
Slc44a5 |
T |
C |
3: 153,964,086 (GRCm39) |
M484T |
probably benign |
Het |
Slc5a1 |
A |
G |
5: 33,318,140 (GRCm39) |
K598E |
probably benign |
Het |
Smc1b |
T |
C |
15: 85,008,003 (GRCm39) |
H258R |
probably benign |
Het |
Smu1 |
T |
C |
4: 40,744,073 (GRCm39) |
D318G |
probably damaging |
Het |
Sned1 |
T |
A |
1: 93,199,406 (GRCm39) |
F495L |
probably damaging |
Het |
Svs3a |
C |
A |
2: 164,131,804 (GRCm39) |
S124Y |
probably damaging |
Het |
Syngr4 |
A |
G |
7: 45,536,464 (GRCm39) |
V186A |
probably benign |
Het |
Tars3 |
G |
A |
7: 65,305,539 (GRCm39) |
M254I |
possibly damaging |
Het |
Tdpoz1 |
T |
A |
3: 93,578,143 (GRCm39) |
R214* |
probably null |
Het |
Tm2d3 |
A |
G |
7: 65,344,987 (GRCm39) |
D54G |
probably damaging |
Het |
Trim66 |
A |
T |
7: 109,074,320 (GRCm39) |
I647N |
probably damaging |
Het |
Triml2 |
T |
A |
8: 43,646,548 (GRCm39) |
W346R |
probably damaging |
Het |
Trp53bp1 |
A |
T |
2: 121,046,545 (GRCm39) |
V1085D |
probably benign |
Het |
Trpv2 |
T |
C |
11: 62,483,612 (GRCm39) |
V483A |
probably benign |
Het |
Ugp2 |
G |
T |
11: 21,278,949 (GRCm39) |
N412K |
probably benign |
Het |
Upf1 |
T |
C |
8: 70,792,004 (GRCm39) |
D418G |
probably null |
Het |
Vmn2r77 |
C |
A |
7: 86,461,152 (GRCm39) |
P826Q |
probably damaging |
Het |
Vrtn |
T |
C |
12: 84,696,936 (GRCm39) |
M562T |
probably benign |
Het |
Wdr55 |
A |
G |
18: 36,895,419 (GRCm39) |
N132S |
possibly damaging |
Het |
Wipf2 |
A |
T |
11: 98,787,040 (GRCm39) |
R356S |
possibly damaging |
Het |
Zdhhc6 |
T |
C |
19: 55,287,228 (GRCm39) |
K411E |
probably benign |
Het |
Zfp260 |
A |
G |
7: 29,804,765 (GRCm39) |
K222E |
probably damaging |
Het |
Zfp280d |
A |
G |
9: 72,220,011 (GRCm39) |
N237S |
probably damaging |
Het |
Zfp445 |
T |
G |
9: 122,682,547 (GRCm39) |
S465R |
possibly damaging |
Het |
Zfp821 |
A |
G |
8: 110,450,979 (GRCm39) |
D324G |
probably damaging |
Het |
|
Other mutations in Slit3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00731:Slit3
|
APN |
11 |
35,512,981 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01324:Slit3
|
APN |
11 |
35,501,529 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01612:Slit3
|
APN |
11 |
35,591,211 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02145:Slit3
|
APN |
11 |
35,520,569 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02146:Slit3
|
APN |
11 |
35,125,675 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02430:Slit3
|
APN |
11 |
35,068,601 (GRCm39) |
splice site |
probably null |
|
IGL02528:Slit3
|
APN |
11 |
35,469,801 (GRCm39) |
missense |
probably benign |
|
IGL02530:Slit3
|
APN |
11 |
35,598,969 (GRCm39) |
makesense |
probably null |
|
IGL02640:Slit3
|
APN |
11 |
35,591,172 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02819:Slit3
|
APN |
11 |
35,062,417 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02839:Slit3
|
APN |
11 |
35,539,874 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL03150:Slit3
|
APN |
11 |
35,399,084 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03161:Slit3
|
APN |
11 |
35,591,241 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03336:Slit3
|
APN |
11 |
35,560,928 (GRCm39) |
missense |
probably damaging |
0.97 |
Bloated
|
UTSW |
11 |
35,524,779 (GRCm39) |
missense |
possibly damaging |
0.55 |
Quellung
|
UTSW |
11 |
35,542,647 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02988:Slit3
|
UTSW |
11 |
35,598,890 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4791001:Slit3
|
UTSW |
11 |
35,552,072 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0013:Slit3
|
UTSW |
11 |
35,598,745 (GRCm39) |
missense |
probably benign |
|
R0013:Slit3
|
UTSW |
11 |
35,598,745 (GRCm39) |
missense |
probably benign |
|
R0334:Slit3
|
UTSW |
11 |
35,469,928 (GRCm39) |
missense |
probably damaging |
0.97 |
R0385:Slit3
|
UTSW |
11 |
35,591,109 (GRCm39) |
missense |
probably damaging |
0.98 |
R0840:Slit3
|
UTSW |
11 |
35,514,263 (GRCm39) |
splice site |
probably benign |
|
R1065:Slit3
|
UTSW |
11 |
35,012,462 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1364:Slit3
|
UTSW |
11 |
35,560,934 (GRCm39) |
missense |
probably benign |
|
R1476:Slit3
|
UTSW |
11 |
35,577,126 (GRCm39) |
missense |
probably damaging |
0.97 |
R1508:Slit3
|
UTSW |
11 |
35,461,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R1665:Slit3
|
UTSW |
11 |
35,125,733 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1692:Slit3
|
UTSW |
11 |
35,550,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R1696:Slit3
|
UTSW |
11 |
35,566,750 (GRCm39) |
missense |
probably damaging |
0.99 |
R1727:Slit3
|
UTSW |
11 |
35,520,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R1752:Slit3
|
UTSW |
11 |
35,455,480 (GRCm39) |
missense |
probably damaging |
0.98 |
R1970:Slit3
|
UTSW |
11 |
35,521,668 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2077:Slit3
|
UTSW |
11 |
35,435,575 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2126:Slit3
|
UTSW |
11 |
35,579,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R2162:Slit3
|
UTSW |
11 |
35,579,509 (GRCm39) |
missense |
probably null |
1.00 |
R2873:Slit3
|
UTSW |
11 |
35,435,620 (GRCm39) |
nonsense |
probably null |
|
R3813:Slit3
|
UTSW |
11 |
35,566,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R3831:Slit3
|
UTSW |
11 |
35,579,509 (GRCm39) |
missense |
probably null |
1.00 |
R3832:Slit3
|
UTSW |
11 |
35,579,509 (GRCm39) |
missense |
probably null |
1.00 |
R3833:Slit3
|
UTSW |
11 |
35,579,509 (GRCm39) |
missense |
probably null |
1.00 |
R3839:Slit3
|
UTSW |
11 |
35,399,064 (GRCm39) |
missense |
probably benign |
0.10 |
R4152:Slit3
|
UTSW |
11 |
35,589,147 (GRCm39) |
missense |
probably damaging |
0.98 |
R4387:Slit3
|
UTSW |
11 |
35,574,875 (GRCm39) |
missense |
probably benign |
0.12 |
R4795:Slit3
|
UTSW |
11 |
35,542,647 (GRCm39) |
critical splice donor site |
probably null |
|
R4910:Slit3
|
UTSW |
11 |
35,523,549 (GRCm39) |
missense |
probably damaging |
0.99 |
R4933:Slit3
|
UTSW |
11 |
35,579,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R5048:Slit3
|
UTSW |
11 |
35,479,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R5106:Slit3
|
UTSW |
11 |
35,503,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R5138:Slit3
|
UTSW |
11 |
35,479,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R5218:Slit3
|
UTSW |
11 |
35,575,002 (GRCm39) |
critical splice donor site |
probably null |
|
R5338:Slit3
|
UTSW |
11 |
35,512,975 (GRCm39) |
missense |
probably benign |
|
R5354:Slit3
|
UTSW |
11 |
35,566,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R5436:Slit3
|
UTSW |
11 |
35,598,738 (GRCm39) |
missense |
probably benign |
0.05 |
R5896:Slit3
|
UTSW |
11 |
35,598,932 (GRCm39) |
missense |
probably damaging |
0.99 |
R5933:Slit3
|
UTSW |
11 |
35,520,578 (GRCm39) |
missense |
probably benign |
0.04 |
R5963:Slit3
|
UTSW |
11 |
35,591,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R5964:Slit3
|
UTSW |
11 |
35,591,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R6125:Slit3
|
UTSW |
11 |
35,461,560 (GRCm39) |
critical splice donor site |
probably null |
|
R6153:Slit3
|
UTSW |
11 |
35,591,310 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6484:Slit3
|
UTSW |
11 |
35,552,125 (GRCm39) |
missense |
probably benign |
|
R6526:Slit3
|
UTSW |
11 |
35,552,119 (GRCm39) |
missense |
probably benign |
0.33 |
R6797:Slit3
|
UTSW |
11 |
35,524,779 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6887:Slit3
|
UTSW |
11 |
35,435,633 (GRCm39) |
splice site |
probably null |
|
R7067:Slit3
|
UTSW |
11 |
35,399,057 (GRCm39) |
missense |
probably benign |
0.04 |
R7150:Slit3
|
UTSW |
11 |
35,461,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R7228:Slit3
|
UTSW |
11 |
35,490,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R7232:Slit3
|
UTSW |
11 |
35,501,516 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7418:Slit3
|
UTSW |
11 |
35,577,255 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7545:Slit3
|
UTSW |
11 |
35,591,139 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7727:Slit3
|
UTSW |
11 |
35,574,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R7820:Slit3
|
UTSW |
11 |
35,591,235 (GRCm39) |
missense |
probably benign |
0.23 |
R8177:Slit3
|
UTSW |
11 |
35,469,919 (GRCm39) |
missense |
probably damaging |
0.99 |
R8179:Slit3
|
UTSW |
11 |
35,554,903 (GRCm39) |
missense |
probably benign |
0.31 |
R8416:Slit3
|
UTSW |
11 |
35,399,062 (GRCm39) |
missense |
probably benign |
0.08 |
R8417:Slit3
|
UTSW |
11 |
35,501,438 (GRCm39) |
missense |
probably damaging |
0.99 |
R8476:Slit3
|
UTSW |
11 |
35,520,596 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8785:Slit3
|
UTSW |
11 |
35,560,968 (GRCm39) |
missense |
probably damaging |
0.98 |
R8955:Slit3
|
UTSW |
11 |
35,589,207 (GRCm39) |
missense |
probably damaging |
0.97 |
R9040:Slit3
|
UTSW |
11 |
35,594,136 (GRCm39) |
missense |
probably damaging |
0.98 |
R9068:Slit3
|
UTSW |
11 |
35,574,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R9088:Slit3
|
UTSW |
11 |
35,012,463 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9266:Slit3
|
UTSW |
11 |
35,598,808 (GRCm39) |
missense |
probably damaging |
0.98 |
R9539:Slit3
|
UTSW |
11 |
35,589,155 (GRCm39) |
nonsense |
probably null |
|
R9636:Slit3
|
UTSW |
11 |
35,594,088 (GRCm39) |
missense |
probably damaging |
0.97 |
X0028:Slit3
|
UTSW |
11 |
35,455,464 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Slit3
|
UTSW |
11 |
35,598,751 (GRCm39) |
nonsense |
probably null |
|
|